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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20520Generated: October 26, 2026

3-[4-(azetidin-1-ylcarbonyl)-2-fluorophenoxy]-5-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethoxy)-N-(5-methylpyrazin-2-yl)benzamide → 3-{[4-(Azetidin-1-ylcarbonyl)-2-fluorophenyl]oxy}-5-{[(1S)-2-hydroxy-1-methylethyl]oxy}-N-(5-methylpyrazin-2-yl)benzamide

https://huagongshe.com/reaction/20520

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[4-(azetidin-1-ylcarbonyl)-2-fluorophenoxy]-5-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethoxy)-N-(5-methylpyrazin-2-yl)benzamideHCID 59346860—
SolventHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
Product3-{[4-(Azetidin-1-ylcarbonyl)-2-fluorophenyl]oxy}-5-{[(1S)-2-hydroxy-1-methylethyl]oxy}-N-(5-methylpyrazin-2-yl)benzamideHCID 11533103—

Reaction Steps

A mixture of 3-[4-(azetidin-1-ylcarbonyl)-2-fluorophenoxy]-5-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethoxy)-N-(5-methylpyrazin-2-yl)benzamide (3.6 g, 5.96 mmol) in methanol (60 mL) and 1M hydrochloric acid (60 mL) was stirred for 30 mins at RT. The volatiles were removed in vacuo and the residue adjusted to pH6 with saturated aqueous sodium bicarbonate solution then extracted into ethyl acetate (3×100 mL). The combined organic layers were washed with water (100 mL), brine (100 mL), dried (MgSO4), filtered and the solvents removed in vacuo. 10% Methanol in ethyl acetate was added and a white solid filtered off. This was crystallised from ethyl acetate/methanol to give the desired compound. (1.24 g), mpt 172° C. The data was in agreement with samples prepared through alternative routes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745475B2
Source datasetuspto-grants-2010_06
ORD IDord-7b44f4c4550c4259a865e69abacb08ca
Source noteuspto-grants-2010_06